JR / Med Qualification & Validation Specialist Qualification & Validation • QbD Spain (Barcelona)

TRIUM Clinical Consulting NV; Barcelona; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A leading company in the life sciences field seeks a Qualification & Validation Specialist to manage multiple projects in the pharmaceutical and medical device sectors. The role involves ensuring compliance and effective validation of various systems and equipment, with an emphasis on continuous learning and teamwork. Join an innovative and positive environment dedicated to quality and personal growth.

Servicios

Attractive salary package

Commitment to job security

Continuous learning and development

Formación

• Eager to contribute to enhancing quality within pharmaceuticals.
• Strong and positive attitude to overcome challenges.
• Open to learning and contributing to innovations.

Responsabilidades

• Support and document validation protocols for lab equipment.
• Collaborate with teams to ensure successful validation.
• Participate in audits and maintain quality records.

Conocimientos

Problem Solving

Collaboration

Adaptability

Educación

Master’s degree in engineering, pharmacy, or chemistry

Descripción del empleo

QbD Groupteam offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices / IVD. We are always looking for the next QbD’er in Qualification & Validation.

What do we expect from you as a Qualification & Validation Specialist?

As a Qualification & Validation specialist, you work on multiple projects in Spain with several organizations within the pharmaceutical or medical device industry. You are responsible for the effective and efficient validation and qualification of lab equipment, cleanrooms, utilities, HVAC systems, GMP production equipment, medical devices, and processes.

• Support equipment qualification activities (IQ / OQ / PQ) in compliance with company policies and regulatory requirements.
• Assist in the preparation, execution, and documentation of validation protocols under supervision.
• Participate in FAT (Factory Acceptance Testing) and SAT (Site Acceptance Testing) for new equipment, supporting test execution and documentation.
• Collaborate with cross-functional teams to ensure successful implementation of validation and qualification tasks.
• Contribute to the development and maintenance of validation lifecycle documentation and ensure traceability of quality records.
• Learn and apply regulatory guidelines (e.g., FDA, EU GMP) related to validation and equipment qualification.
• Participate in the review of technical documentation and ensure data integrity across validation activities.
• Support internal and external audits by organizing documentation and providing responses to audit queries.
• Show interest in continuous improvement and quality systems, actively engaging in training and mentoring opportunities.

Who are we looking for?

• Education: You hold a Master’s degree in engineering, technological sciences, pharmacy, or chemistry. Whether you’re an industrial engineer, civil engineer, bioengineer, industrial pharmacist, or have a background in biomedical sciences, biotechnology, biochemistry, or chemistry, we want to meet you!

Passion: You’ve completed your studies and are eager to contribute to enhancing quality within the pharmaceutical, biotechnological, and health sectors. Join forces with over 600 fellow consultants.

A true QbD’er can be recognized by the following qualities:

• Resilient: Your strong and positive attitude helps you overcome any challenge.
• Hungry for knowledge: You are always open to learning.
• No non-sense mentality: You can be straightforward in a respectful way.
• Innovative: You are constantly looking for new and better solutions.
• Not too serious: Your job is serious, but you don’t take yourself too seriously.

What’s in it for you?

• QbD Group offers you an attractive and competitive salary package that will be tailored to individual needs, considering legal requirements and local laws and regulations.
• Join us to build a sustainable career, where job security is ensured, and lasting, meaningful connections are formed.
• As we’re a knowledge-based company, you’re guaranteed to embark on a continuous journey of learning and development.
• Be part of our global success story. As an award-winning company, we value everyone’s contribution and celebrate achievements together.

Our promise to you:

• As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.
• Moreover, we aim to create a joyful community where you dare to be and can be yourself. Because the best way to grow is by growing together as unique individuals.
• In short … We stand for? JPEG : Joy in Partnership, going the extra mile to get things done!

Interested? Send us your CV and motivation letter and who knows, we might welcome you soon into our QbD family!

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